Canonical Allele Identifier: CA992471840
Gene: GRIN3B HGNC NCBI

Linked Data

dbSNP Id: rs10666583
gnomAD v3: 19-1004897-G-GTT
gnomAD v4: 19-1004897-G-GTT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004897_1004898insTT , CM000681.2:g.1004897_1004898insTT GRCh38
NC_000019.9:g.1004896_1004897insTT , CM000681.1:g.1004896_1004897insTT GRCh37
NC_000019.8:g.955896_955897insTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234389.3:c.1396_1397insTT MANE Select ENSP00000234389.3:p.Gly466ValfsTer?
ENST00000588335.1:n.146_147insTT
NM_138690.1:c.1396_1397insTT NP_619635.1:p.Gly466ValfsTer?
NM_138690.2:c.1396_1397insTT NP_619635.1:p.Gly466ValfsTer?
XM_017026243.2:c.-183_-182insTT XP_016881732.1:n.-183_-182insTT
NM_138690.3:c.1396_1397insTT MANE Select NP_619635.1:p.Gly466ValfsTer?
Search 100 bp 5'
Search 100 bp 3'